HGVS | Genome Assembly |
---|---|
NC_000004.12:g.35981489C>A , CM000666.2:g.35981489C>A | GRCh38 |
NC_000004.11:g.35983111C>A , CM000666.1:g.35983111C>A | GRCh37 |
NC_000004.10:g.35659506C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000503225.5:n.1607+3741G>T | ||
XR_925192.1:n.1460G>T |